ENST00000477151.2:n.89G>T
|
|
|
ENST00000643794.1:c.102G>T
|
ENSP00000495765.1:p.Arg34Ser
|
|
ENST00000651669.1:c.7-106G>T
MANE Select
|
ENSP00000499044.1:n.7-106G>T
|
|
ENST00000368567.4:c.7-106G>T
|
ENSP00000357555.4:n.7-106G>T
|
|
ENST00000392558.4:c.7-106G>T
|
ENSP00000376341.4:n.7-106G>T
|
|
ENST00000477151.1:n.136G>T
|
|
|
ENST00000493224.5:n.247G>T
|
|
|
NM_001030.4:c.7-106G>T
|
NP_001021.1:n.7-106G>T
|
|
NM_001030.6:c.7-106G>T
MANE Select
|
NP_001021.1:n.7-106G>T
|
|
NM_001349946.1:c.-116G>T
|
NP_001336875.1:n.-116G>T
|
|
NM_001349947.1:c.-116G>T
|
NP_001336876.1:n.-116G>T
|
|
NM_001349946.2:c.-116G>T
|
NP_001336875.1:n.-116G>T
|
|
NM_001349947.2:c.-116G>T
|
NP_001336876.1:n.-116G>T
|
|